Quality of Life and Cardiometabolic Risk Factors in Patients After Debanding

This study is ongoing, but not recruiting participants.
Sponsor:
Information provided by (Responsible Party):
Markus Mueller, University of Zurich
ClinicalTrials.gov Identifier:
NCT00497627
First received: July 5, 2007
Last updated: July 8, 2013
Last verified: July 2013
  Purpose

Follow up of debanding patients


Condition
Bariatric Patients

Study Type: Observational
Official Title: Quality of Life and Cardiometabolic Risk Factors in Patients After Debanding

Further study details as provided by University of Zurich:

Primary Outcome Measures:
  • Quality of Life [ Time Frame: 2 to 5 years after debanding ] [ Designated as safety issue: No ]

Enrollment: 12
Study Start Date: January 2007
Estimated Study Completion Date: December 2013
Estimated Primary Completion Date: December 2013 (Final data collection date for primary outcome measure)
Detailed Description:

Follow up of debanding patients regarding cardiometabolic risk factors

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population

Follow up of debanding patients regarding cardiometabolic risk factors

Criteria

Inclusion criteria:

  • Previous debanding after lap. gastric bypass

Exclusion criteria:

  • Further bariatric procedures
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00497627

Locations
Switzerland
University Hospital of Zurich
Zurich, Switzerland
Sponsors and Collaborators
University of Zurich
Investigators
Study Director: 01 Studienregister MasterAdmins UniversitaetsSpital Zuerich
  More Information

No publications provided

Responsible Party: Markus Mueller, PD Dr. med., University of Zurich
ClinicalTrials.gov Identifier: NCT00497627     History of Changes
Other Study ID Numbers: StV 38-2006
Study First Received: July 5, 2007
Last Updated: July 8, 2013
Health Authority: Switzerland: Swissmedic

ClinicalTrials.gov processed this record on July 26, 2014